Abstract: A shoulder can include a fixed bearing having a generally spherical articulating surface configured to be coupled to a glenoid. The implant can also include a floating bearing member defining a first spherical bearing surface and a second planar articulating bearing surface. The implant can include a stem defining a stem planar bearing surface coupled to the second planar articulating bearing surface. The second planar articulating bearing surface can cooperate with the stem planar bearing surface to enable the floating bearing to translate relative to the stem.

Abstract: A reverse modular humeral implant for implantation into a humerus that includes a natural humeral shaft and a natural humeral head. The implant includes a humeral stem implantable into the natural humeral shaft, and an adapter couplable to the humeral stem, the adapter including an anchoring projection configured to be coupled to a convex bearing.

Abstract: A shoulder implant assembly constructed in accordance to one example of the present disclosure includes a frame member, a cup, and a glenosphere. The frame member can have a central hub and a first arm extending therefrom. The frame member can be configured to selectively and alternatively couple with first shoulder implant components in a traditional shoulder configuration and with second shoulder implant components in a reverse shoulder configuration. The cup can have a concave surface that is configured to articulate with a humeral head component. The cup can be selectively coupled to the frame member in the traditional shoulder configuration. The glenosphere can have an outer articulating surface that is configured to articulate with a second cup. The glenosphere can be selectively coupled to the frame member in the reverse shoulder configuration.

Abstract: A glenoid prosthetic is provided and may include a first component having an articulating surface engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of the first component than the articulating surface. A second component may be attached to the first component proximate to the engagement surface and may be attached to a resected glenoid of a scapula. The second component may be formed from a different material than the first component and may include at least one coupling stem received within an aperture formed in the resected glenoid.

Abstract: A method for preparing an implant having a porous metal component. A loose powder mixture including a biocompatible metal powder and a spacing agent is prepared and compressed onto a metal base. After being compressed, the spacing agent is removed, thereby forming a compact including a porous metal structure pressed on the metal base. The compact is sintered, forming a subassembly, which is aligned with a metal substrate portion of an implant. A metallurgical bonding process, such as diffusion bonding, is performed at the interface of the subassembly and the metal substrate to form an implant having a porous metal component.

Abstract: An orthopedic device includes a femoral implant having a non-custom internal bone engagement surface. The femoral implant includes at least nine parameters adjusted preoperatively to correspond to a specific patient. The parameters can include patient-specific lengths, such as, for example, medial and lateral condyle widths and notch height, and patient-specific medial and lateral angles.

Abstract: An orthopedic device includes a first patient-specific element having a first patient-specific surface preoperatively configured to mate and conform to a first anatomic portion of a specific patient based on medical scans of the patient. The orthopedic device includes a second patient-specific element having a second patient-specific surface preoperatively configured to mate and conform to a second anatomic portion of a specific patient based on medical scans of the patient. An arcuate bridge couples the first and second patient-specific portions. The arcuate bridge is configured to provide clearance the patient's anatomy between the first and second anatomic portions.

Abstract: A system and method of implanting a distal wrist implant relative to a host bone is presented. A distal radial component having a body including a first connection portion couplable to a stem is coupled to a second prosthetic coupled to a medial surface of the body. The second prosthetic replaces at least a portion of the sigmoid notch.

Abstract: A method of implanting a knee replacement system in a leg with a femur and a tibia of a patient can include, implanting a femoral component onto a condyle of the femur and placing a trial tibial component on a tibial plateau of the tibia. The tension of a posterior cruciate ligament can be adjusted. The tension of an anterior cruciate ligament can be adjusted. The posterior position of the trial tibial component can be adjusted. The knee condition at toe off onset can be simulated during walking.

Abstract: A system for compressing a fracture can include a first bone plate having a first proximal end and a first distal end, and a second bone plate having a second proximal end and a second distal end. The second bone plate can be spaced apart from the first bone plate. The system can include an expansion member coupled to the second proximal end of the second bone plate. The movement of the expansion member relative to the second bone plate can cause the first distal end of the first bone plate and the second distal end of the second bone plate to move toward each other to compress the fracture.

Abstract: A method and apparatus of performing a procedure relative to the glenohumeral joint. Resection of the glenoid and/or the humerus can proceed through an incision formed near the glenohumeral joint. The incision can be formed generally near a superior-lateral portion near the glenohumeral joint and allow less invasive access to the glenohumeral joint and the portions that form the glenohumeral joint. The procedure can be performed with no or little detaching of the subscapularis, and with no or little dislocating of the glenohumeral joint.

Abstract: A prosthesis to replace a portion of the anatomy, such as the humerus, can include a first shell. A second prosthesis can be positioned relative to the shell to provide the bearing surface to articulate with a glenoid prosthesis or glenoid. The second prosthesis can include a connection portion to engage a connection portion in the shell.

Abstract: A method and apparatus for positioning an implant system in anatomy is disclosed. The apparatus can include an alignment member operable to contact an implant portion, a bone, or other appropriate portion. The method can include using the apparatus to assist in positioning a single or multi-piece implant member. Also, a method of aligning a first implant position relative to another implant position is disclosed.